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Relation of FGFR2 Genetic Polymorphisms to the Association Between Oral Contraceptive Use and the Risk of Breast Cancer in Chinese Women

机译:FGFR2基因多态性与口服避孕药使用与中国女性乳腺癌风险之间的关系

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摘要

The fibroblast growth factor receptor 2 gene (FGFR2) has been associated with the risk of breast cancer in multiple ethnic populations, and its effect has been suggested to be hormone-dependent. A large, 2-stage, population-based case-control study was conducted in urban Shanghai, China, during the periods of 1996–1998 and 2002–2005. Exposure and genotyping information from 2,073 patients with breast cancer and 2,084 age-matched population controls was available for evaluation of the interactions between FGFR2 polymorphisms and exogenous estrogen exposure in the development of breast cancer. A logistic regression model was used to compute adjusted odds ratios and 95% confidence intervals. Of 20 genotyped and 25 imputed single nucleotide polymorphisms (SNPs), 22 were significantly associated with breast cancer. Three genotyped SNPs in close linkage disequilibrium, rs2303568, rs3135730, and rs1078806, and an imputed SNP of rs755793 in complete linkage disequilibrium with other 8 SNPs were observed to interact significantly with oral contraceptive (OC) use. The SNP-cancer association was evident only among OC users, and the OC use was only associated with the risk of breast cancer among carriers of these minor alleles at these loci. These findings suggest that genetic variants in FGFR2 may modify the role of OC use in causing breast cancer in Chinese women.
机译:成纤维细胞生长因子受体2基因(FGFR2)与多个族裔人群患乳腺癌的风险有关,其作用被认为是激素依赖性的。在1996-1998年和2002-2005年期间,在中国上海市区进行了大规模的,基于人群的,分为两个阶段的病例对照研究。来自2,073名乳腺癌患者和2,084个年龄匹配的人群对照的暴露和基因分型信息可用于评估乳腺癌发展过程中FGFR2多态性与外源性雌激素暴露之间的相互作用。使用逻辑回归模型计算调整后的优势比和95%置信区间。在20个基因型和25个估算的单核苷酸多态性(SNP)中,有22个与乳腺癌显着相关。观察到紧密连锁不平衡的三种基因型SNP,rs2303568,rs3135730和rs1078806,以及推定的rs755793的SNP与其他8种SNP完全连锁不平衡,与口服避孕药(OC)的使用显着相互作用。仅在OC使用者中,SNP-癌症关联才明显,并且在这些基因座上,这些次要等位基因携带者中,OC的使用仅与患乳腺癌的风险有关。这些发现表明,FGFR2的遗传变异可能会改变OC的使用在中国女性乳腺癌中的作用。

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